ISO9001 CoV-19 Antigen Influenza Rapid Test Kit For Healthcare Workers

Product Specification

Rapid Test Kit CoV-19 Antigen And Influenza A/b Comprehensive Rapid Test Kit 20 Tests Professional Test Rapid Test Kit

Intended Use
SARS-CoV-2 Antigen & influenza A/B Rapid Test Kit provideds a simple, rapid detection as an aid in the differential diagnosis of SARS-CoV-2 Antigen and Influenza A&B using nasal swab specimens. This easy-to-use product and rapid results can be used for the screening  of early infected  patients and asymptomatic patients. It also effective supplement for nucleic acid detection.
Specification

Main Components

• 20 Test cassettes
• 2 Sample extraction buffers
• 20 Sample tubes
• 20 Swabs
• 1 Tube Stand
• 1 Instruction Manaual

Use  Step

• Take out the test cassette from the sealed pouch, place it on a clean and level surface with the sample port well up.

• Apply 2 full drops of the treated sample (60μl-70μl) vertically into each of the two sample wells of the test cassette.

• Observe the test results immediately within 15~20 minutes, the result is invalid over 20 minutes.

 
Interpretation Of Result

• POSITIVE: The presence of T (T on nCoV /A or B on Flu) and C lines within the reaction window indicate a positive result on SARS-CoV-2 or Flu A and/or B infection or co-infection.

• NEGATIVE: One colored line appears in the control region(C). No apparent colored line appears in the test region (T on nCoV /A or B on Flu). The negative result does not indicate the absence of analytes in the sample, it only indicates the level of tested analytes in the sample is less than the minimum detection limit

• INVALID: No colored lines appear, or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.

 
Feature

• Results ready in 15minutes
• Easy to administer and read results
• Affordable, no need for instrument, highly portable
• Enable testing on a massive scale
• For healthcare workers use only

Limitation

• This reagent is a qualitative detection reagent, which cannot determine the exact content of antigen.
• The test results of this reagent are only for the reference of clinicians and should not be taken as the sole basis for clinical diagnosis and treatment. Clinical management of patients should be considered in the light of their symptoms/signs, medical history, other laboratory tests and treatment responses.
• Restricted by antigen detection reagent method, the lowest detection limit (sensitivity analysis) is generally lower than that of nucleic acid detection, so the researchers deal with negative result to give more attention, should be combined with other test results comprehensive judgment, advice to doubt the negative result of nucleic acid detection or virus isolation culture identification method for review.
• False negative results may be caused by unreasonable sample collection, transport and treatment, and low viral load in samples.

FAQ

• About MOQ?

We have the limit order which is 10000, we would like to cooperate with you, don't worry about MOQ, just send us of your what items you want order.

• What is your lead time?

 Stock 3-7 days in general. Or please contact us by email for specific lead time base on your order quantities.

• Accept OEM or ODM order?

Yes, we accept both OEM and ODM for customers.

• What are your terms of delivery?

We can accept EXW, FOB, CIF, etc. You can choose one which is the most convenient for you.

• Manufacturer or Trade Company?

We're Manufacturer.